Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Accsl |
A |
T |
2: 93,696,589 (GRCm39) |
|
probably benign |
Het |
Adam30 |
G |
A |
3: 98,070,222 (GRCm39) |
S685N |
probably benign |
Het |
Adamts12 |
T |
C |
15: 11,071,843 (GRCm39) |
V129A |
probably benign |
Het |
Agxt2 |
T |
C |
15: 10,373,837 (GRCm39) |
F81S |
probably damaging |
Het |
Ahnak2 |
A |
T |
12: 112,749,409 (GRCm39) |
I186N |
probably damaging |
Het |
Amz1 |
A |
T |
5: 140,737,691 (GRCm39) |
|
probably null |
Het |
Anapc5 |
G |
A |
5: 122,926,481 (GRCm39) |
A619V |
possibly damaging |
Het |
Aoc1l3 |
C |
A |
6: 48,967,173 (GRCm39) |
P707H |
probably damaging |
Het |
Bbox1 |
T |
C |
2: 110,095,956 (GRCm39) |
D336G |
probably damaging |
Het |
Bivm |
A |
G |
1: 44,165,942 (GRCm39) |
T131A |
probably benign |
Het |
Bpi |
A |
T |
2: 158,109,660 (GRCm39) |
I203F |
probably benign |
Het |
Cd151 |
A |
C |
7: 141,050,569 (GRCm39) |
T241P |
probably damaging |
Het |
Cdh20 |
G |
A |
1: 109,988,862 (GRCm39) |
V255I |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,148,171 (GRCm39) |
|
probably benign |
Het |
Cul9 |
C |
G |
17: 46,833,101 (GRCm39) |
A1326P |
probably damaging |
Het |
Dclre1b |
A |
C |
3: 103,711,192 (GRCm39) |
S240A |
probably benign |
Het |
Ddc |
A |
C |
11: 11,796,634 (GRCm39) |
|
probably null |
Het |
Dkk1 |
T |
C |
19: 30,524,650 (GRCm39) |
R252G |
probably damaging |
Het |
Dmrtc2 |
T |
A |
7: 24,573,738 (GRCm39) |
M191K |
possibly damaging |
Het |
Eml6 |
A |
G |
11: 29,699,824 (GRCm39) |
S1771P |
possibly damaging |
Het |
Emx1 |
T |
C |
6: 85,165,353 (GRCm39) |
|
probably benign |
Het |
Fah |
T |
C |
7: 84,250,344 (GRCm39) |
M1V |
probably null |
Het |
Fmo6 |
A |
T |
1: 162,753,710 (GRCm39) |
M144K |
probably damaging |
Het |
Frem1 |
A |
G |
4: 82,868,589 (GRCm39) |
V1445A |
probably benign |
Het |
Fsd2 |
T |
C |
7: 81,209,518 (GRCm39) |
D108G |
probably benign |
Het |
Gfm2 |
A |
G |
13: 97,301,708 (GRCm39) |
|
probably null |
Het |
Ghrhr |
T |
A |
6: 55,365,254 (GRCm39) |
L416* |
probably null |
Het |
Glipr1l2 |
C |
A |
10: 111,919,371 (GRCm39) |
L31I |
possibly damaging |
Het |
Gpr149 |
A |
G |
3: 62,511,888 (GRCm39) |
L37P |
probably damaging |
Het |
Hoxa9 |
A |
G |
6: 52,202,693 (GRCm39) |
I131T |
probably damaging |
Het |
Htra4 |
T |
C |
8: 25,520,635 (GRCm39) |
D342G |
possibly damaging |
Het |
Idh1 |
G |
T |
1: 65,200,319 (GRCm39) |
N348K |
probably benign |
Het |
Impdh2 |
T |
C |
9: 108,439,028 (GRCm39) |
F99S |
probably benign |
Het |
Kank4 |
T |
C |
4: 98,653,806 (GRCm39) |
Y874C |
probably damaging |
Het |
Kazn |
A |
T |
4: 141,886,349 (GRCm39) |
|
probably benign |
Het |
Kcnq3 |
T |
A |
15: 65,871,891 (GRCm39) |
T593S |
probably benign |
Het |
Lamc1 |
T |
C |
1: 153,122,977 (GRCm39) |
|
probably benign |
Het |
Magi3 |
A |
G |
3: 103,968,946 (GRCm39) |
|
probably null |
Het |
Map3k19 |
A |
G |
1: 127,751,617 (GRCm39) |
V578A |
probably benign |
Het |
Meox2 |
T |
C |
12: 37,159,151 (GRCm39) |
C108R |
possibly damaging |
Het |
Nlrp9c |
C |
A |
7: 26,079,860 (GRCm39) |
C722F |
probably damaging |
Het |
Or2a5 |
T |
C |
6: 42,874,285 (GRCm39) |
V300A |
probably benign |
Het |
Pde10a |
C |
T |
17: 9,139,378 (GRCm39) |
|
probably benign |
Het |
Ppfia4 |
A |
G |
1: 134,260,021 (GRCm39) |
|
probably benign |
Het |
Psg18 |
T |
C |
7: 18,088,742 (GRCm39) |
M1V |
probably null |
Het |
Qtrt1 |
A |
G |
9: 21,323,782 (GRCm39) |
T136A |
probably benign |
Het |
Retsat |
T |
C |
6: 72,580,634 (GRCm39) |
|
probably benign |
Het |
Rxfp2 |
T |
C |
5: 149,975,021 (GRCm39) |
V210A |
probably benign |
Het |
Sfswap |
G |
A |
5: 129,584,207 (GRCm39) |
|
probably null |
Het |
Slc16a7 |
A |
T |
10: 125,067,241 (GRCm39) |
L133I |
possibly damaging |
Het |
Slc30a3 |
A |
T |
5: 31,244,154 (GRCm39) |
M376K |
probably damaging |
Het |
Spmip4 |
T |
A |
6: 50,566,121 (GRCm39) |
K118M |
probably damaging |
Het |
Srbd1 |
C |
T |
17: 86,405,940 (GRCm39) |
C620Y |
probably null |
Het |
Trip10 |
T |
A |
17: 57,560,363 (GRCm39) |
L100Q |
probably damaging |
Het |
Tyrp1 |
C |
T |
4: 80,763,105 (GRCm39) |
Q331* |
probably null |
Het |
Vangl2 |
G |
T |
1: 171,832,353 (GRCm39) |
T501N |
probably damaging |
Het |
Vdr |
A |
T |
15: 97,767,214 (GRCm39) |
Y185N |
probably benign |
Het |
Vmn1r123 |
C |
T |
7: 20,896,257 (GRCm39) |
P50S |
probably damaging |
Het |
Vmn1r158 |
T |
A |
7: 22,489,870 (GRCm39) |
H113L |
probably benign |
Het |
Vmn2r12 |
A |
T |
5: 109,240,720 (GRCm39) |
I131N |
probably benign |
Het |
Vmn2r72 |
T |
A |
7: 85,401,152 (GRCm39) |
E89V |
probably damaging |
Het |
Xrcc6 |
A |
G |
15: 81,915,364 (GRCm39) |
D94G |
probably damaging |
Het |
Zbtb32 |
T |
A |
7: 30,290,692 (GRCm39) |
E201V |
possibly damaging |
Het |
Zfp185 |
A |
T |
X: 72,042,929 (GRCm39) |
E138D |
possibly damaging |
Het |
Zmynd11 |
T |
A |
13: 9,739,585 (GRCm39) |
H437L |
probably damaging |
Het |
|
Other mutations in Gm19965 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0993:Gm19965
|
UTSW |
1 |
116,749,555 (GRCm39) |
missense |
probably benign |
0.04 |
R1016:Gm19965
|
UTSW |
1 |
116,749,031 (GRCm39) |
nonsense |
probably null |
|
R1175:Gm19965
|
UTSW |
1 |
116,748,550 (GRCm39) |
splice site |
probably benign |
|
R1335:Gm19965
|
UTSW |
1 |
116,732,349 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1773:Gm19965
|
UTSW |
1 |
116,748,989 (GRCm39) |
nonsense |
probably null |
|
R1802:Gm19965
|
UTSW |
1 |
116,748,633 (GRCm39) |
nonsense |
probably null |
|
R2884:Gm19965
|
UTSW |
1 |
116,749,313 (GRCm39) |
missense |
probably benign |
0.14 |
R3435:Gm19965
|
UTSW |
1 |
116,749,353 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4072:Gm19965
|
UTSW |
1 |
116,748,801 (GRCm39) |
missense |
probably benign |
0.17 |
R4585:Gm19965
|
UTSW |
1 |
116,749,508 (GRCm39) |
missense |
probably benign |
0.00 |
R4801:Gm19965
|
UTSW |
1 |
116,749,626 (GRCm39) |
missense |
probably benign |
|
R4802:Gm19965
|
UTSW |
1 |
116,749,626 (GRCm39) |
missense |
probably benign |
|
R5328:Gm19965
|
UTSW |
1 |
116,749,148 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5856:Gm19965
|
UTSW |
1 |
116,749,579 (GRCm39) |
missense |
probably benign |
|
R5960:Gm19965
|
UTSW |
1 |
116,749,201 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6185:Gm19965
|
UTSW |
1 |
116,749,003 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6297:Gm19965
|
UTSW |
1 |
116,750,410 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6374:Gm19965
|
UTSW |
1 |
116,750,021 (GRCm39) |
missense |
probably benign |
0.06 |
R6811:Gm19965
|
UTSW |
1 |
116,731,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R6860:Gm19965
|
UTSW |
1 |
116,748,609 (GRCm39) |
missense |
probably benign |
0.19 |
R7076:Gm19965
|
UTSW |
1 |
116,749,005 (GRCm39) |
missense |
|
|
R7162:Gm19965
|
UTSW |
1 |
116,750,095 (GRCm39) |
missense |
unknown |
|
R7290:Gm19965
|
UTSW |
1 |
116,748,921 (GRCm39) |
missense |
|
|
R7473:Gm19965
|
UTSW |
1 |
116,749,602 (GRCm39) |
missense |
unknown |
|
R7643:Gm19965
|
UTSW |
1 |
116,749,959 (GRCm39) |
missense |
unknown |
|
R7919:Gm19965
|
UTSW |
1 |
116,749,850 (GRCm39) |
nonsense |
probably null |
|
R8187:Gm19965
|
UTSW |
1 |
116,749,532 (GRCm39) |
nonsense |
probably null |
|
R8306:Gm19965
|
UTSW |
1 |
116,749,515 (GRCm39) |
missense |
|
|
R8477:Gm19965
|
UTSW |
1 |
116,730,854 (GRCm39) |
start gained |
probably benign |
|
R8751:Gm19965
|
UTSW |
1 |
116,749,867 (GRCm39) |
missense |
unknown |
|
R8876:Gm19965
|
UTSW |
1 |
116,749,776 (GRCm39) |
missense |
unknown |
|
R9151:Gm19965
|
UTSW |
1 |
116,748,942 (GRCm39) |
missense |
|
|
R9389:Gm19965
|
UTSW |
1 |
116,749,566 (GRCm39) |
missense |
|
|
R9444:Gm19965
|
UTSW |
1 |
116,732,393 (GRCm39) |
missense |
|
|
R9696:Gm19965
|
UTSW |
1 |
116,749,210 (GRCm39) |
missense |
|
|
R9696:Gm19965
|
UTSW |
1 |
116,730,838 (GRCm39) |
start gained |
probably benign |
|
Z1088:Gm19965
|
UTSW |
1 |
116,732,330 (GRCm39) |
missense |
probably benign |
0.30 |
|